Skip to main content

Table 2 Demographic, clinical and laboratory parameters of the study population

From: Predictive value of pentraxin-3 on disease severity and mortality risk in patients with hemorrhagic fever with renal syndrome

Ā 

Grouping according to the clinical type

Grouping according to the prognosis

Mild-type (nĀ =ā€‰17)

Moderate-type (nĀ =ā€‰27)

Severe-type (nĀ =ā€‰26)

Critical-type (nĀ =ā€‰35)

Healthy controls (nĀ =ā€‰27)

Ļ‡2/F/H

P value

Survivors (nĀ =ā€‰91)

Non-survivors (nĀ =ā€‰14)

Ļ‡2/t/Z

P value

Gender

ā€ƒFemale

6 (35.3%)

5 (18.5%)

3 (11.5%)

7 (20.0%)

6 (22.2%)

3.690

0.450

17 (20.7%)

3 (21.4%)

0.004

0.953

ā€ƒMale

11 (64.7%)

22 (81.5%)

23 (88.5%)

28 (80.0%)

21 (77.8%)

65 (79.3%)

11 (78.6%)

Age, years

36.47ā€‰Ā±ā€‰17.14

40.07ā€‰Ā±ā€‰13.67

43.62ā€‰Ā±ā€‰12.96

44.51ā€‰Ā±ā€‰15.09

40.65ā€‰Ā±ā€‰13.16

1.419

0.242

41.76ā€‰Ā±ā€‰14.34

46.57ā€‰Ā±ā€‰16.52

āˆ’1.136

0.259

a Timing, days

7.0 (5.0ā€“7.5)

6.0 (5.0ā€“7.0)

6.0 (5.0ā€“7.0)

6.0 (5.0ā€“8.0)

ā€“

1.036

0.793

7.0 (5.0ā€“8.0)

6.0 (4.5ā€“6.5)

āˆ’1.643

0.058

Hospital stay, days

ā€ƒAll patients

10.00ā€‰Ā±ā€‰2.15

13.72ā€‰Ā±ā€‰3.41

20.42ā€‰Ā±ā€‰5.95

17.32ā€‰Ā±ā€‰11.81

ā€“

6.771

<ā€‰0.001

16.0 (12.0ā€“23.0)

6.0 (1.76ā€“10.5)

āˆ’4.999

<ā€‰0.001

ā€ƒSurvivors

10.00ā€‰Ā±ā€‰2.15

13.72ā€‰Ā±ā€‰3.41

20.42ā€‰Ā±ā€‰5.95

26.41ā€‰Ā±ā€‰7.13

ā€“

34.549

<ā€‰0.001

Pentraxin-3, ng/mL

ā€ƒAcute phase

58.21 (22.84ā€“334.37)

216.13 (63.61ā€“539.01)

171.07 (51.28ā€“458.82)

570.30 (138.37ā€“1088.51)

0.46 (0.18ā€“0.65)

69.128

<ā€‰0.001

181.79 (41.14ā€“518.53)

935.04 (258.74ā€“1453.42)

āˆ’3.021

0.003

ā€ƒConvalescent phase

2.52 (1.25ā€“11.19)

11.30 (5.64ā€“26.90)

5.87 (3.14ā€“8.00)

4.92 (2.49ā€“11.34)

56.540

<ā€‰0.001

ā€“

ā€“

ā€“

ā€“

WBC, Ɨā€‰109/L

11.60 (7.86ā€“13.34)

11.08 (7.67ā€“16.72)

13.37 (8.91ā€“20.16)

14.95 (9.62ā€“27.72)

ā€“

6.019

0.111

12.49 (8.45ā€“18.15)

33.05 (12.04ā€“46.58)

āˆ’2.886

0.004

PLT, Ɨ109/L

58.50 (50.25ā€“104.50)

37.00 (25.50ā€“55.50)

34.00 (22.75ā€“51.50)

26.00 (14.00ā€“54.50)

ā€“

11.966

0.008

39.50 (24.00ā€“58.25)

22.50 (10.25ā€“39.50)

āˆ’2.938

0.003

ALB, g/L

31.31ā€‰Ā±ā€‰3.96

29.30ā€‰Ā±ā€‰4.43

28.22ā€‰Ā±ā€‰6.01

27.17ā€‰Ā±ā€‰4.67

ā€“

2.008

0.120

28.86ā€‰Ā±ā€‰5.06

23.81ā€‰Ā±ā€‰8.21

2.227

0.042

ALT, U/L

37.50 (28.75ā€“59.00)

43.00 (28.25ā€“68.75)

53.00 (42.75ā€“88.50)

64.00 (49.00ā€“118.00)

ā€“

8.149

0.043

51.00 (32.00ā€“78.50)

97.00 (55.50ā€“265.50)

āˆ’3.081

0.002

AST, U/L

69.50 (47.25ā€“105.50)

81.00 (56.00ā€“112.75)

89.50 (60.50ā€“154.00)

121.00 (69.00ā€“197.00)

ā€“

5.582

0.134

85.00 (59.00ā€“124.00)

260.50 (185.00ā€“825.75)

āˆ’4.543

<ā€‰0.001

PT, sec

10.90 (10.63ā€“11.70)

11.50 (9.75ā€“12.20)

11.50 (10.60ā€“13.05)

11.50 (10.80ā€“13.20)

ā€“

1.710

0.635

11.50 (10.60ā€“12.40)

15.10 (12.53ā€“21.00)

āˆ’3.982

<ā€‰0.001

APTT, sec

34.22ā€‰Ā±ā€‰5.02

37.17ā€‰Ā±ā€‰7.48

41.22ā€‰Ā±ā€‰9.77

35.49ā€‰Ā±ā€‰8.03

ā€“

2.873

0.042

36.00 (31.90ā€“43.00)

58.50 (41.95ā€“75.20)

āˆ’4.341

<ā€‰0.001

Fib, g/L

2.97ā€‰Ā±ā€‰0.91

2.49ā€‰Ā±ā€‰0.72

2.77ā€‰Ā±ā€‰1.02

2.26ā€‰Ā±ā€‰1.01

ā€“

1.861

0.144

2.62ā€‰Ā±ā€‰0.93

1.54ā€‰Ā±ā€‰0.76

4.104

<ā€‰0.001

BUN, mmol/L

8.86ā€‰Ā±ā€‰4.92

14.54ā€‰Ā±ā€‰9.06

19.55ā€‰Ā±ā€‰11.01

19.78ā€‰Ā±ā€‰6.94

ā€“

5.699

0.001

13.97 (7.07ā€“22.99)

13.27 (7.61ā€“29.90)

āˆ’0.426

0.670

Cr, Ī¼mol/L

112.40 (66.15ā€“213.65)

175.60 (85.50ā€“333.90)

303.10 (122.40ā€“540.15)

431.30 (248.65ā€“533.00)

ā€“

16.075

0.001

216.35 (109.63ā€“481.75)

245.25 (97.10ā€“327.78)

āˆ’0.405

0.686

  1. Abbreviations: WBC White blood cells, PLT Platelets, ALB Albumin, ALT Alanine aminotransferase, AST Aspartate aminotransferase, PT Prothrombin time, APTT Activated partial thromboplastin time, Fib Fibrinogen, BUN Blood urea nitrogen, Cr Creatinine, sec Second
  2. aTiming: Timing of blood collection druingthe acute phase, duration from illness onset to the day of blood collection